Literature DB >> 914279

LBA technique in the detection of chromosome variants. II. Chromosomes except for those with Q variants.

Y Nakagome, S Oka, E Matsunaga.   

Abstract

In Part I of this communication, a technique (LBA) was described which used DNA replication in the evaluation of chromosome variants in man. It was shown that the method was very useful in the detection of variants in D- and G-group chromosomes. Results on pars 3 and 4 were also presented. In Part II, the rest of chromosomes were examined. In the evaluation of qh variants in 1, 9 and 16, the LBA technique proved itself to be a very effective implement. It was practically free of technical variables coherent with C-band technique and, therefore, it was possible to use the size of an euchromatic segment of a chromosome as a reference standard. LBA variants were observed in about 50% of the members of the remaining 12 pairs of chromosomes, i.e., 2, 5, 6, 7, 8, 10, 11, 12, 17, 18, 19, and 20.

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Year:  1977        PMID: 914279     DOI: 10.1007/bf00402157

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  13 in total

1.  Initiation of DNA replication in human chromosomes.

Authors:  Y Nakagome
Journal:  Exp Cell Res       Date:  1977-05       Impact factor: 3.905

2.  Human Q and C chromosomal variations: distribution and incidence.

Authors:  W H McKenzie; H A Lubs
Journal:  Cytogenet Cell Genet       Date:  1975

3.  Pitfalls in the use of chromosome variants for paternity dispute cases.

Authors:  Y Nakagome; T Kitagawa; K Iinuma; E Matsunaga; T Shinoda
Journal:  Hum Genet       Date:  1977-07-26       Impact factor: 4.132

4.  Polymorphism of human C-band heterochromatin. I. Frequency of variants.

Authors:  A P Craig-Holmes; F B Moore; M W Shaw
Journal:  Am J Hum Genet       Date:  1973-03       Impact factor: 11.025

5.  An analysis of the technical variables in the production of C bands.

Authors:  W H McKenzie; H A Lubs
Journal:  Chromosoma       Date:  1973       Impact factor: 4.316

6.  Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over.

Authors:  A P Craig-Holmes; F B Moore; M W Shaw
Journal:  Am J Hum Genet       Date:  1975-03       Impact factor: 11.025

7.  Letter: Cd banding of human chromosomes observed in the C-banding procedure.

Authors:  T Abe; M Morita; K Kawai
Journal:  Lancet       Date:  1975-11-15       Impact factor: 79.321

8.  Late replicating bands of human chromosomes demonstrated by fluorochrome and Giemsa staining.

Authors:  K H Grzeschik; M A Kim; R Johannsmann
Journal:  Humangenetik       Date:  1975-08-29

9.  Variation in human acrocentric chromosomes with acridine orange reverse banding.

Authors:  R S Verma; H A Lubs
Journal:  Humangenetik       Date:  1975-09-20

10.  Frequency of chromosomal fluorescence polymorphism in normal persons and in clinical patients with diagnosed chromosome aberrations.

Authors:  E Schwinger; H Wehner
Journal:  Hum Genet       Date:  1976-05-19       Impact factor: 4.132

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  6 in total

1.  A rare heteromorphism of chromosome 20 and reproductive loss.

Authors:  D R Romain; S Whyte; D F Callen; H J Eyre
Journal:  J Med Genet       Date:  1991-07       Impact factor: 6.318

2.  Variation in chromosome 19.

Authors:  H A Gardner; E M Wood
Journal:  J Med Genet       Date:  1979-02       Impact factor: 6.318

3.  LBA technique in the detection of chromosome variants. I. Chromosomes with known sites of Q variants.

Authors:  S Oka; Y Nakagome; E Matsunaga; M Arima
Journal:  Hum Genet       Date:  1977-11-02       Impact factor: 4.132

4.  A new approach in the evaluation of chromosome variants in man. II. Pairs without Q or C (qh) variants.

Authors:  J Azumi; Y Nakagome; S Oka; E Matsunaga
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

5.  A new approach in the evaluation of chromosome variants in man, III. Pairs with established Q or C variable sites.

Authors:  S Oka; Y Nakagome; J Azumi; E Matsunaga; Y Igarashi
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

Review 6.  Pericentric inversions. Problems and significance for clinical genetics.

Authors:  P Kaiser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

  6 in total

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